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Paclitaxel
Paclitaxel - 47351-009-50 - (Paclitaxel)
Drug Information of Paclitaxel
| Product NDC: | 47351-009 |
| Proprietary Name: | Paclitaxel |
| Non Proprietary Name: | Paclitaxel |
| Active Ingredient(s): | 6 mg/mL & nbsp; Paclitaxel |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Paclitaxel
| Product NDC: | 47351-009 |
| Labeler Name: | Onco Therapies Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091540 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110930 |
Package Information of Paclitaxel
| Package NDC: | 47351-009-50 |
| Package Description: | 50 mL in 1 VIAL (47351-009-50) |
NDC Information of Paclitaxel
| NDC Code | 47351-009-50 |
| Proprietary Name | Paclitaxel |
| Package Description | 50 mL in 1 VIAL (47351-009-50) |
| Product NDC | 47351-009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Paclitaxel |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110930 |
| Marketing Category Name | ANDA |
| Labeler Name | Onco Therapies Limited |
| Substance Name | PACLITAXEL |
| Strength Number | 6 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Microtubule Inhibition [PE],Microtubule Inhibitor [EPC] |
